Jonathan M. Scott1, Matthew C. Murphy1, Arvin Arani1, Christopher G. Schwarz1, Armando Manduca1, John Huston III1, and Richard L. Ehman1
1Radiology, Mayo Clinic, Rochester, MN, United States
Synopsis
Magnetic Resonance Elastography stiffness
estimates in intracranial tumors correlate with intraoperative assessment of
tumor consistency, but the spatial kernel-based stiffness calculation of Direct
Inversion (DI) creates challenges for small or heterogeneous tumors. The
objective of this study is to evaluate an artificial neural network based
inversion technique (NNI) in the assessment of small stiff inclusions in a
brain phantom. This study shows that NNI can resolve inclusions as small as
1.75cm in diameter with a contrast to noise ratio higher than that of DI. Furthermore,
preliminary clinical results show agreement with intraoperative findings.
Introduction
Magnetic
Resonance Elastography (MRE) is an MRI-based technique for noninvasive assessment
of tissue stiffness1. When intracranial tumors are resected, tumor stiffness
is an important determinate of surgical difficulty and preoperative knowledge
of tumor consistency may have implications on the chosen surgical approach. Two
studies have shown MRE tumor stiffness values correlate with intraoperative
surgical assessments of meningioma consistency, but the spatial kernel-based
nature of stiffness calculation in MRE creates challenges in spatial resolution
for small or heterogeneous tumors2,3. The objective of this study was to evaluate
the capabilities of a recently-developed neural network-based inversion (NNI)4
to aid the assessment of small stiff inclusions within a brain phantom.Methods
Image acquisition.
MRE was performed on a polyvinyl
chloride (PVC) brain phantom with background stiffness of ~3.5kPa (at 60Hz) embedded
with 6 spherical inclusions (~7.0kPa at 60Hz) ranging in size from 1.75-3cm at
driver power levels of 3, 5, and 7 percent. Two scans were completed at each
power level. Scanning was performed on a compact 3T system with a high performance gradient capable of
80 mT/m amplitude and 700
T/m/s5-7 slew rate using a modified 3D GRE pulse sequence
with parameters as follows: 7.2 mT/m motion encoding gradients (MEG),
mechanical vibration=60Hz, TE=20.4ms, TR=24.1ms, first-moment nulled MEG,
motion encoding sensitivity (MENC) = 7.1 μm/rad, BW = ±25kHz, FOV =
240x240x192mm3, acquisition matrix= 120x120x96, resolution = 2x2x2mm3,
flip angle = 12°, 2D ARC reduction=2, 8 channel receiver array (Invivo,
Gainesville Fl), scan time = 12:25. One patient with a meningioma (recruited
under an IRB-approved protocol) was imaged using the same scan parameters.
Data analysis. After
computing the curl of the displacement field, smoothing was performed with a
3x3x3 quartic filter8 and stiffness was estimated by algebraic
direct inversion (DI)9. A 3x3x3 median filter was applied to these
stiffness maps to remove outliers. To train the neural network, 1.2 million
7x7x7 simulated data sets were generated with 2-mm isotropic voxels and 4 phase
offsets evenly distributed over one period of 60Hz motion. The stiffness of
each cube varied randomly between 0.1 and 10 kPa. Sinusoidal waves of the
appropriate wavelength were computed from up to 10 point-sources outside of the
cube. Noise was added such that the signal to noise ratio varied from 1 to 20
for each example. Model features were the real and imaginary parts of the first
harmonic of the curled data selected from a structural element with the same spatial
footprint as DI prior to median filtering. An artificial neural network
consisting of 3 hidden layers with 24 nodes in each and hyperbolic tangent
transfer functions was trained using scaled conjugate gradient backpropagation10
on 1 million of the simulated datasets, the rest being used for validation. To
prevent overfitting, training was stopped when mean-squared error failed to
improve in six consecutive iterations in the validation set. When applying NNI
to image data, the same features as above for each curl component were fed to
NNI, and the final stiffness map (elastogram) was generated as the weighted sum
of squares of these images. Contrast to noise ratio was defined as11:
$$CNR=\sqrt{\frac{2 (median_{inclusion} - median_{background})^2}{({σ_{inclusion}}^2+{σ_{background}}^2 )}}$$
For NNI the statistics were calculated
directly from the elastogram. For DI, the median and standard deviation were
calculated from the filtered map.
Results
Elastograms of the PVC phantom with
inclusions as generated by DI and NNI are shown in Figure 1. All six inclusions
in the phantom could be visualized with both inversions. Stiffness estimates
from DI were globally lower than for NNI. CNR for the first run of the middle
power level is shown in Figure 2. Results were similar for all runs of all
power levels. NNI provided higher CNR in 18/18 possible combinations of driver
power and inclusion size. Figure 3 shows NNI and DI elastograms in a patient
with a meningioma. At resection, this tumor was found to be very stiff and
fibrous. The NNI elastogram of this tumor better demonstrates the margins and high
level of stiffness than the DI elastogram and provided a better match to
intraoperative findings.Conclusions
This study shows that artificial neural
networks provide a promising alternative inversion method for MRE. While both
NNI and DI were able to resolve inclusions as small as 1.75 cm in diameter, NNI
provided higher CNR in 18/18 combinations of inclusion size and driver power
level. Preliminary clinical results in using this inversion to assess
focal brain lesions are promising.Acknowledgements
This research was supported by National Institutes of Health R01 grant EB001981 (R.L.E). References
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